Data / Drug companies / Non-Standardized House Dust Allergenic Extract
Non-Standardized House Dust Allergenic Extract drugs: 1 drug from 8 companies in the FDA NDC directory
Non-Standardized House Dust Allergenic Extract is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 19 products in this class from 8 companies, covering 1 drug by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on October 2, 2025.
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- 8Companies
- 19Products
- 1Drugs by generic name
Drugs in the Non-Standardized House Dust Allergenic Extract class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| House dust | 2 | 2 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Newton Laboratories, Inc. | 8 | liquid; pellet | Unapproved homeopathic products | September 25, 2023 |
| Nutritional Specialties, Inc. | 3 | spray | Unapproved homeopathic products | October 2, 2025 |
| Apex Energetics Inc. | 2 | solution/ drops | Unapproved homeopathic products | March 15, 1993 |
| Professional Complementary Health Formulas | 2 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Allermed Laboratories, Inc. | 1 | injection | Biologics (BLA) | March 12, 1974 |
| BioActive Nutritional, Inc. | 1 | liquid | Unapproved homeopathic products | June 21, 2022 |
| Dna Labs, Inc. | 1 | solution | Unapproved homeopathic products | January 1, 1990 |
| Energique, Inc. | 1 | liquid | Unapproved homeopathic products | March 24, 2020 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Liquid | 9 | 47.4% |
| Spray | 3 | 15.8% |
| Pellet | 3 | 15.8% |
| Solution/ drops | 2 | 10.5% |
| Injection | 1 | 5.3% |
| Solution | 1 | 5.3% |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.